Selective Tissue Penetration of the Corneal Layers of Cyclosporin 2% Associated with Miglyol in Rabbits.

IF 1.9 4区 医学 Q2 OPHTHALMOLOGY Journal of Ocular Pharmacology and Therapeutics Pub Date : 2025-01-20 DOI:10.1089/jop.2024.0087
Gladys Gress, Fabien Lamoureux, Julien Bourgain, Ariella Ganem, Christophe Arnoult, Julie Gueudry, Marc Muraine
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Abstract

Purpose: Cyclosporin A (CsA) is a drug used to prevent immune rejection in corneal transplantation. Most grafts performed today are endothelial grafts which are complicated with poor penetration of CsA into the endothelium due to its hydrophobicity. To improve CsA penetration into the corneal a new ocular formulation of CsA 2% with Miglyol was developed and is commercially available. The purpose of this pharmacokinetic study was to determine the concentrations of CsA in all layers of the cornea, in particular in the endothelium after topical administration of CsA 2%-Miglyol in rabbits. Methods: Sixteen rabbits were divided in 4 groups according to the time from the last instillation of CsA 2%-Miglyol to corneal sampling. Rabbit eyes received one drop of CsA twice a day for 5 days. Corneal tissue and plasma samples were collected at 2, 6, 12, and 24 h. CsA concentrations were measured using liquid chromatography-tandem mass spectrometry method. Results: Maximum concentrations (Cmax) of CsA were obtained in corneal tissues within 2 h after the last instillation of CsA 2%-Miglyol, except in the endothelium (12 h). Cmax were 59.75 ± 12.09 ng/mg, 15.66 ± 4.31 ng/mg, 5.17 ± 0.88 ng/mg, and 2.65 ± 0.47 ng/mg for the epithelium, endothelium, anterior stroma and posterior stroma. CsA concentrations remained high over a 24-h in all corneal layers. Conclusions: The topical application of CsA 2%-Miglyol allowed a high concentration of CsA in the corneal endothelium. The good penetration of CsA into the endothelium suggests that this formulation can be effective to prevent endothelial graft rejection.

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2%环孢素对兔角膜层的选择性穿透作用。
目的:环孢素A (Cyclosporin A, CsA)是一种预防角膜移植免疫排斥反应的药物。目前进行的大多数移植是内皮移植,由于其疏水性,CsA渗透到内皮细胞的能力较差。为了提高CsA对角膜的渗透,我们开发了一种新的CsA 2%米糠醇眼部配方,并已上市。本药代动力学研究的目的是测定兔角膜各层CsA的浓度,特别是局部给予CsA 2%-米盖尔醇后内皮的浓度。方法:16只家兔按最后一次注射2%米糠醇CsA至角膜取样时间分为4组。兔眼滴注CsA 1滴,每天2次,连续5天。分别于第2、6、12和24小时采集角膜组织和血浆样品。采用液相色谱-串联质谱法测定CsA浓度。结果:除内皮细胞(12 h)外,其余角膜组织(上皮、内皮、前间质和后间质)Cmax分别为59.75±12.09 ng/mg、15.66±4.31 ng/mg、5.17±0.88 ng/mg和2.65±0.47 ng/mg。所有角膜层的CsA浓度在24小时内保持高水平。结论:局部应用2%米盖尔醇CsA可使角膜内皮细胞内CsA浓度升高。CsA在内皮中的良好渗透表明该制剂可有效预防内皮移植排斥反应。
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来源期刊
CiteScore
4.60
自引率
4.30%
发文量
72
审稿时长
1 months
期刊介绍: Journal of Ocular Pharmacology and Therapeutics is the only peer-reviewed journal that combines the fields of ophthalmology and pharmacology to enable optimal treatment and prevention of ocular diseases and disorders. The Journal delivers the latest discoveries in the pharmacokinetics and pharmacodynamics of therapeutics for the treatment of ophthalmic disorders. Journal of Ocular Pharmacology and Therapeutics coverage includes: Glaucoma Cataracts Retinal degeneration Ocular infection, trauma, and toxicology Ocular drug delivery and biotransformation Ocular pharmacotherapy/clinical trials Ocular inflammatory and immune disorders Gene and cell-based therapies Ocular metabolic disorders Ocular ischemia and blood flow Proliferative disorders of the eye Eyes on Drug Discovery - written by Gary D. Novack, PhD, featuring the latest updates on drug and device pipeline developments as well as policy/regulatory changes by the FDA.
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